Trojan GOAT 3ct 00022600800132Recalls & reported problems
Church & Dwight CO., Inc. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00022600800132), received between Nov 3, 2025 and Nov 3, 2025 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 3, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THIS SPONTANEOUS CASE WAS REPORTED BY A CONSUMER FROM THE UNITED STATES OF AMERICA VIA SMS MESSAGING. THE REPORTER (CONSUMER) REPORTED USING TROJAN GOAT NON-LATEX CONDOM. AS PER THE REPORTER, "AFTER USING A CONDOM FROM THIS PACK I GOT INFECTION AND IRRITATION. HOW DO I RETURN THIS?" NO ADDITIONAL INFORMATION WAS AVAILABLE. MEDICAL HISTORY AND CONCOMITANT MEDICATION - UNKNOWN. NOTE: CHURCH AND DWIGHT, EMAILED CONSUMER THE ADE SURVEY LINK TO COMPLETE. IN ADDITION, CONSUMER WAS ASKED "ANY MEDICAL TREATMENT RECEIVED? WHAT TYPE OF INFECTION DID YOU EXPERIENCE?". AWAITING ADDITIONAL INFORMATION; HOWEVER, THE CASE WAS CONSERVATIVELY ASSESSED AS SERIOUS (REPORTABLE) WITH LIMITED INFORMATION ON INFECTION.
Patient problems: Unspecified Infection
MAUDE report 23447680 ↗
Other Condom, synthetic devices
- SKYN 7412Suretex Limited - Branch · Condom, Synthetic1 report
- Trojan Supra™ Premium Condoms Non-Latex Bareskin™ 00022600902423Church & Dwight CO., Inc. · Condom, synthetic1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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